Clinical and imaging “red flags” for the diagnosis of multiple system atrophy lookalikes-Reference-Cited by-同舟云学术

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Clinical and imaging “red flags” for the diagnosis of multiple system atrophy lookalikes

Published:2023-07 Issue: Volume:112 Page:105372
ISSN:1353-8020
Container-title:Parkinsonism & Related Disorders
language:en
Short-container-title:Parkinsonism & Related Disorders

Author:

Gallo Silvia,Ory-Magne Fabienne,Le-Traon Anne Pavy,Rascol Olivier,Debs Rachel,Leung Clémence,Fabbri Margherita^ORCID

Publisher

Elsevier BV

Subject

Neurology (clinical),Geriatrics and Gerontology,Neurology

Reference9 articles.

1. Second consensus statement on the diagnosis of multiple system atrophy;Gilman;Neurology,2008

2. ANO10 mutational screening in recessive ataxia: genetic findings and refinement of the clinical phenotype;Nanetti;J. Neurol.,2019

3. ANO10 Function in Health and Disease;Chrysanthou,2022

4. Autosomal recessive cerebellar ataxia type 3 due to ANO10 mutations: delineation and genotype-phenotype correlation study;Renaud;JAMA Neurol.,2014

5. The movement disorder society criteria for the diagnosis of multiple system atrophy, movement disorders;Wenning;Off. J. Movement. Dis. Soc.,2022

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